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Poor sleep and shift work associate with increased blood pressure and inflammation in UK Biobank participants.
Kanki, Monica; Nath, Artika P; Xiang, Ruidong; Yiallourou, Stephanie; Fuller, Peter J; Cole, Timothy J; Cánovas, Rodrigo; Young, Morag J.
Afiliação
  • Kanki M; Cardiovascular Endocrinology Laboratory, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
  • Nath AP; Department of Medicine (Alfred Health), Central Clinical School, Monash University, Clayton, VIC, Australia.
  • Xiang R; Cambridge-Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
  • Yiallourou S; Cambridge-Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
  • Fuller PJ; Turner Institute for Brain and Mental Health, Department of Central Clinical School, Monash University, Clayton, VIC, Australia.
  • Cole TJ; Centre of Endocrinology and Metabolism, Hudson Institute of Medical Research, Clayton, VIC, Australia.
  • Cánovas R; Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
  • Young MJ; Cambridge-Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Nat Commun ; 14(1): 7096, 2023 11 04.
Article em En | MEDLINE | ID: mdl-37925459
ABSTRACT
Disrupted circadian rhythms have been linked to an increased risk of hypertension and cardiovascular disease. However, many studies show inconsistent findings and are not sufficiently powered for targeted subgroup analyses. Using the UK Biobank cohort, we evaluate the association between circadian rhythm-disrupting behaviours, blood pressure (SBP, DBP) and inflammatory markers in >350,000 adults with European white British ancestry. The independent U-shaped relationship between sleep length and SBP/DBP is most prominent with a low inflammatory status. Poor sleep quality and permanent night shift work are also positively associated with SBP/DBP. Although fully adjusting for BMI in the linear regression model attenuated effect sizes, these associations remain significant. Two-sample Mendelian Randomisation (MR) analyses support a potential causal effect of long sleep, short sleep, chronotype, daytime napping and sleep duration on SBP/DBP. Thus, in the current study, we present a positive association between circadian rhythm-disrupting behaviours and SBP/DBP regulation in males and females that is largely independent of age.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Jornada de Trabalho em Turnos / Distúrbios do Início e da Manutenção do Sono Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Jornada de Trabalho em Turnos / Distúrbios do Início e da Manutenção do Sono Idioma: En Ano de publicação: 2023 Tipo de documento: Article